Results 171 to 180 of about 28,766 (211)
Merkel cell carcinoma with synchronous but spatially distinct squamous cell carcinoma of the head: Case report of differing PRAME expression and response to checkpoint inhibitor therapy. [PDF]
JAAD Case RepAbbott CB +4 more
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Impact of UV Exposure and Incidence of Merkel Cell Carcinoma Between 1990 and 2018 in Austria. [PDF]
Cancers (Basel)Erovic BM +6 more
europepmc +1 more source
Line-Field Confocal Optical Coherence Tomography in Merkel Cell Carcinoma and Histopathological Correlation. [PDF]
Dermatol Pract ConceptGreco ME +5 more
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Merkel Cell Carcinoma: Evolving Therapeutics, Continued Challenges. [PDF]
Head NeckHolley HA +6 more
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Hematology/Oncology Clinics of North America, 2007
Merkel cell carcinoma (MCC) is a rare and extremely aggressive skin cancer that arises from primary neural cells. It presents most commonly in the elderly and immunocompromised patients. Pathologically, MCC should be distinguished from extrapulmonary small cell lung cancer or metastatic small cell lung cancer or a small cell variant of melanoma.
Vy, Dinh +3 more
openaire +2 more sources
Merkel cell carcinoma (MCC) is a rare and extremely aggressive skin cancer that arises from primary neural cells. It presents most commonly in the elderly and immunocompromised patients. Pathologically, MCC should be distinguished from extrapulmonary small cell lung cancer or metastatic small cell lung cancer or a small cell variant of melanoma.
Vy, Dinh +3 more
openaire +2 more sources
Current Treatment Options in Oncology, 2004
Merkel cell carcinoma is a rare cutaneous neoplasm most commonly affecting the head and neck of elderly white patients. Even with treatment, Merkel cell carcinoma has a strong propensity toward local recurrence, lymphatic spread, and distant metastasis. Because of its rarity and the subsequent lack of well-controlled clinical trials, no single standard
Michael S, Lehrer +2 more
openaire +4 more sources
Merkel cell carcinoma is a rare cutaneous neoplasm most commonly affecting the head and neck of elderly white patients. Even with treatment, Merkel cell carcinoma has a strong propensity toward local recurrence, lymphatic spread, and distant metastasis. Because of its rarity and the subsequent lack of well-controlled clinical trials, no single standard
Michael S, Lehrer +2 more
openaire +4 more sources
Seminars in Oncology, 2007
Merkel cell carcinoma (MCC) is a rare, aggressive cutaneous cancer that predominately affects elderly Caucasians with fair skin and has a propensity for local recurrence and regional lymph node metastases. A variety of terms have been used to describe this tumor, including trabecular cell carcinoma, neuroendocrine or primary small cell carcinoma of the
Michael Howard, Swann, Jaeyoung, Yoon
openaire +2 more sources
Merkel cell carcinoma (MCC) is a rare, aggressive cutaneous cancer that predominately affects elderly Caucasians with fair skin and has a propensity for local recurrence and regional lymph node metastases. A variety of terms have been used to describe this tumor, including trabecular cell carcinoma, neuroendocrine or primary small cell carcinoma of the
Michael Howard, Swann, Jaeyoung, Yoon
openaire +2 more sources
International Journal of Oral and Maxillofacial Surgery, 1992
A case of Merkel cell carcinoma of the cheek is described, highlighting the clinical behaviour, diagnosis and management of this uncommon tumour.
K, Altman, P J, Mahaffey
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A case of Merkel cell carcinoma of the cheek is described, highlighting the clinical behaviour, diagnosis and management of this uncommon tumour.
K, Altman, P J, Mahaffey
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Journal of the American Academy of Dermatology, 1993
Merkel cell carcinoma is a malignant neuroendocrine tumor with features of epithelial differentiation. Biologically aggressive, it may be difficult to diagnose and, particularly in its late stages, even more difficult to treat effectively. This article addresses what is known and what is still controversial about the histogenesis, diagnosis, and ...
D, Ratner +3 more
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Merkel cell carcinoma is a malignant neuroendocrine tumor with features of epithelial differentiation. Biologically aggressive, it may be difficult to diagnose and, particularly in its late stages, even more difficult to treat effectively. This article addresses what is known and what is still controversial about the histogenesis, diagnosis, and ...
D, Ratner +3 more
openaire +2 more sources